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New Blogs
Check out our blog stories below! Be sure to subscribe to be notified of new stories.
If you would like to submit your blog, please send it to info@lupusgreaterohio.org.
Click one of the stories below to read the words of a lupus patient.
Getting the Most Out of Your Relationship with Your Lupus Doctor
How to Get the Most Out of Your Relationship with Your Lupus Doctor By Maria J Antonelli, MD A person finds himself or herself in a vulnerable position when they seek medical care. They are asking for advice on what is going on with their body, figuring out their...
Our Trip to Capitol Hill
2024 National Advocacy Summit By Suzanne Tierney, Lupus Patient First The 2024 National Lupus Advocacy Summit was held in Washington D.C. from May 19th through May 21st. The purpose of the Summit is to bring lupus warriors together from all over the country to learn...
Spring Cleaning Tips
Spring Cleaning Tips for Life with a Chronic Illness Life with a chronic illness is hard. Lupus patients often have fatigue, joint pain, strained ligaments, muscular pain, headaches, and a host of other symptoms. These symptoms often interfere with daily life. Many...
Growing With Lupus
Being diagnosed at a young age has been a lot for me during my life - some good and some bad. The diagnosis itself has caused my life not to go the way I planned or thought, but it’s surely helped me grow over time. I was diagnosed with SLE at 18. I was unable to...
Living Fit With lupus
Pursuing Fitness As a Lupus Patient Living with lupus poses unique challenges, especially when it comes to maintaining physical activity. The pain and fatigue associated with this autoimmune disease can make exercise seem like an uphill battle. However, incorporating...
Assistance Programs For Patients!
Lupus Foundation of America, Greater Ohio Chapter Assistance Programs The LFA, GOC’s Assistance Programs were created as a response to a needs assessment survey of lupus warriors in the state of Ohio. The results showed that lupians would benefit from some help with...
Why is Lupus Difficult to Diagnose?
Causes of Diagnosis Delay For many people with lupus, the average diagnosis delay is six years from the onset of symptoms. Misdiagnosis with another condition often contributes to the time delay before establishment of a proper diagnosis of lupus. The symptoms of...
Creating a Lupus Flare Plan to Manage Your Disease
Lupus Overview Systemic lupus erythematosus is a complex chronic autoimmune condition in which the body’s immune system goes awry. Instead of focusing on attacking foreign invaders like viruses and bacteria, the immune system begins attacking the body’s own cells and...
Avoid The Winter Blues!
It’s the middle of January. You’re still reeling from the chaos of a busy holiday season. Temperatures haven’t climbed above 30 degrees for weeks, and the color outside has alternated between gray and black for what seems like an eternity. Winter has sunk its claws...
THANK YOU WARRIORS!
As we wrap up our 2023 Walk to End Lupus NOW season, we cannot help but be thankful! Thank you to all of our constituents across the state that came out to support us this year. Our Columbus and Cleveland walks raised $80,000 that will now help fund things...